Inhibitors | Comment | Organism | Structure |
---|---|---|---|
S-17092 | i.e. (2S,3aS,7aS)-1-[(R,R)-2-phenylcyclopropyl]-2-[(thiazolidin-3-yl)carbonyl]octahydro-1H-indole, specific enzyme inhibitor | Flavobacterium sp. |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
urotensin II + H2O | Flavobacterium sp. | human substrate, cleavage at the canonical post-proline site | ? | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Flavobacterium sp. | - |
- |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
benzyloxycarbonyl-Gly-Pro-4-nitroanilide + H2O | - |
Flavobacterium sp. | benzyloxycarbonyl-Gly-Pro + 4-nitroaniline | - |
? | |
peptide QATVGDVNTDRPGLLDLK + H2O | i.e. octadecaneuropeptide ODN, the biologically active fragment of diazepam-binding inhibitor, the Ala2 residue is preferred by the enzyme for cleavage, while the Pro-Gly bind is not cleaved, overview | Flavobacterium sp. | TVGDVNTDRPGLLDLK + GDVNTDRPGLLDLK + QA + QATV | - |
? | |
urotensin II + H2O | human substrate, cleavage at the canonical post-proline site | Flavobacterium sp. | ? | - |
? |
Synonyms | Comment | Organism |
---|---|---|
prolyl endopeptidase | - |
Flavobacterium sp. |
Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|
37 | - |
assay at | Flavobacterium sp. |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
7.5 | - |
assay at | Flavobacterium sp. |